1

Ngs Variant Interpretation Jobs (NOW HIRING)

Provide bioinformatics support to include somatic and germline variant calling and analysis, single ... NGS analysis (whole-exome, whole-genome, RNA-seq, ChIP-Seq, both long- and short-read technologies ...

Provide bioinformatics support to include somatic and germline variant calling and analysis, single ... NGS analysis (whole-exome, whole-genome, RNA-seq, ChIP-Seq, both long- and short-read technologies ...

Genome Analyst

Indianapolis, IN · On-site

$78K - $88K/yr

Manages variant databases and monitors day-to-day operations of the literature searching and triage ... Experience in analyzing and interpreting next-generation sequencing (NGS) data * Familiarity with ...

New

Provide bioinformatics support to include somatic and germline variant calling and analysis, single ... NGS analysis (whole-exome, whole-genome, RNA-seq, ChIP-Seq, both long- and short-read technologies ...

next page

Showing results 1-20

Ngs Variant Interpretation information

See salary details

$20.5K

$83.3K

$147K

How much do ngs variant interpretation jobs pay per year?

As of Jul 14, 2026, the average yearly pay for ngs variant interpretation in the United States is $83,348.00, according to ZipRecruiter salary data. Most workers in this role earn between $49,000.00 and $111,000.00 per year, depending on experience, location, and employer.

What is NGS variant interpretation?

NGS variant interpretation is the process of analyzing genetic variants identified through Next-Generation Sequencing (NGS) technology to determine their potential impact on health, disease, or traits. This involves filtering, annotating, and classifying variants according to established guidelines, such as those from the American College of Medical Genetics and Genomics (ACMG). Professionals in this field use bioinformatics tools and databases to interpret the clinical significance of genetic changes and often communicate their findings to clinicians or researchers for decision-making in healthcare or research settings.

What is the difference between Ngs Variant Interpretation vs Genetic Counselor?

AspectNgs Variant InterpretationGenetic Counselor
Required CredentialsCertification in genetics or molecular diagnostics, often a laboratory certificationMaster's degree in genetics, counseling, or related field; certification (ABGC, NSGC)
Work EnvironmentLaboratory setting, analyzing genetic data and variantsClinical setting, providing patient counseling and education
Industry UsageUsed primarily in diagnostic labs and research institutionsUsed in hospitals, clinics, and healthcare facilities
Primary FocusInterpreting genetic variants from NGS dataCommunicating genetic information and implications to patients

While Ngs Variant Interpretation specialists focus on analyzing and interpreting genetic data within laboratories, Genetic Counselors work directly with patients to explain genetic information and its health implications. Both roles require a strong understanding of genetics but serve different functions within the healthcare and diagnostics industry.

What are some of the main challenges faced when interpreting NGS variants, and how can professionals address them?

One of the main challenges in NGS variant interpretation is distinguishing between benign and pathogenic variants, especially when dealing with variants of uncertain significance (VUS). Professionals must stay updated with the latest research, utilize comprehensive databases, and collaborate closely with geneticists, clinicians, and bioinformaticians to ensure accurate interpretation. Regular participation in multidisciplinary team meetings and continuous professional development are essential for overcoming these challenges and delivering clinically actionable insights.

What are the key skills and qualifications needed to thrive as an NGS Variant Interpretation Specialist, and why are they important?

To thrive as an NGS Variant Interpretation Specialist, you need a solid background in genetics, molecular biology, and bioinformatics, often supported by an advanced degree in a life science field. Familiarity with next-generation sequencing (NGS) platforms, databases like ClinVar and HGMD, and analysis tools such as GATK and ANNOVAR is typically required. Strong analytical thinking, attention to detail, and effective communication skills help in interpreting complex genomic data and conveying findings to clinicians or researchers. These skills are crucial for ensuring accurate variant classification, supporting clinical decision-making, and advancing personalized medicine.
More about Ngs Variant Interpretation jobs
What cities are hiring for Ngs Variant Interpretation jobs? Cities with the most Ngs Variant Interpretation job openings:
What states have the most Ngs Variant Interpretation jobs? States with the most job openings for Ngs Variant Interpretation jobs include:
Infographic showing various Ngs Variant Interpretation job openings in the United States as of July 2026, with employment types broken down into 100% Full Time. Highlights an 100% In-person job distribution, with an average salary of $83,348 per year, or $40.1 per hour.
Biomedical Technician - Genomics Core

Biomedical Technician - Genomics Core

CEDARS-SINAI

Sacramento, CA • On-site

$27 - $35.75/hr

Full-time

This job post has expired today. Applications are no longer accepted.


Cedars-Sinai rating

8.6

Company rating: 8.6 out of 10

Based on 130 frontline employees who took The Breakroom Quiz

37th of 1,020 rated hospitals


Job description

Job Description

The Applied Genomics, Computation & Translational Core is looking for a Biomedical Technician to join the team! 

Candidates with experience in single-cell and spatial assay technologies are highly desirable. This includes familiarity with techniques such as single-cell RNA sequencing (scRNA-seq), spatial transcriptomics, multiplex imaging, and other high-dimensional molecular profiling platforms. A working knowledge of sample preparation workflows, library preparation, quality control metrics, and data generation associated with next-generation sequencing or imaging-based assays is strongly valued. Experience handling complex biological specimens and maintaining rigorous data integrity within high-throughput experimental environments is also preferred.

The Cedars-Sinai Applied Genomics, Computation & Translational (AGCT) Core is an automated, high-throughput genomics facility equipped with the latest next-generation sequencing technologies. We specialize in single-cell and spatial omics, utilizing platforms including 10x Genomics (Chromium X, Xenium Analyzer, Visium CytAssist), Parse Biosciences, Scale Biosciences, Illumina, Singular Genomics G4X , and Bruker CosMX SMI. We also offer expertise in long-read sequencing via Oxford Nanopore Technologies (PromethION 24, MinION) and high-throughput short-read sequencing on the Illumina NovaSeq X Plus. We provide comprehensive support covering sample preparation, library construction, and diverse sequencing applications including bulk cell RNA-Seq, WGS/WES, ATAC-Seq, and metagenomics. 

The AGCT Core also delivers extensive bioinformatics analysis. Standard pipelines are established for primary data processing across all services, encompassing read alignment, quality control, expression quantification, variant calling, and peak calling. We also provide downstream analysis packages to help analyze these data in the context of the researcher’s experimental design. We actively collaborate with investigators to develop sophisticated or custom computational solutions for specific research questions, including advanced analysis for spatial transcriptomics data. Our bioinformatics support extends to results interpretation, generation of publication-ready figures, and drafting manuscript methodology.

To learn more please visit Applied Genomics, Computation & Translational Core | Cedars-Sinai. 

Are you ready to be a part of breakthrough research? 

The AGCT Core Biomedical Technician contributes to the laboratory sciences team of the lab. They work independently as part of a team under direct supervision of a team lead.  The Biomedical Technician is responsible for performing laboratory benchwork strictly according to Standard Operating Procedures with accurate documentation and a theoretical understanding of assays utilized.  They perform quality control on RNA and DNA samples, understanding the nuances of sample quality and qualifications.  The Biomedical Technician contributes to the success of projects by providing good oral and written communication, documentation, and attentiveness to detail. They work with state-of-the-art technologies and instruments, performing next generation sequencing library preparation and sequencing.

Primary Duties and Responsibilities:

  • Performs a variety of project-specific process development tasks for multiple clients following standard operating procedures (SOPs).
  • Maintains good documentation in laboratory notebooks, data record/transfer, SOPs, and batch records.
  • Drafts standard operating procedures and maintains computer database.
  • Verifies samples received, logs samples into systems, and may transport to appropriate environment within the facility for storage following SOPs.
  • Performs lab maintenance duties, including glassware cleaning and sterilization.
  • Maintains lab equipment and related records.
  • Prepares cGMP production room, maintains material inventories, and places orders for equipment and supplies.
  • Assists in the operation of specialized equipment and machinery.
  • Ensures all activities comply with regulatory guidelines and safety standards, as appropriate.

Department Specific Responsibilities:

  • Construction of next generation sequencing libraries for bulk cell, single cell, and/or spatial omics using commercially available reagent kits.
  • Illumina short-read sequencing and/or Oxford Nanopore Technologies long-read sequencing of NGS libraries.
  • DNA/RNA QC via fluorescent quantification and automated electrophoresis.
  • Operation of state-of-the-art genomics equipment including NGS sequencers, automated liquid handlers, and tissue imagers, as well as standard laboratory equipment such as thermal cyclers, centrifuges, and qPCR machines.
  • Mathematical calculations, including fold dilution, normalization, and conversions.
  • Understand, analyze, and interpret DNA/RNA/NGS library/sequencing QC results. 
  • Liaise with post-doctoral, doctoral, and staff researchers, clinical investigators, and principal investigators to provide quality customer service.
  • Handle multiple demands and/or manage complex and competing priorities, pivoting as needed based on current needs in a dynamic environment.
  • Apply advanced knowledge of science/learning/specialized intellectual instructions to analyze, interpret, or make deductions from varying facts or circumstances.
  • Provide and/or support a level of work excellence and accuracy; recognize and address flaws or errors that others may overlook.
  • Regular oral and written communication with team members and team lead.
  • Accurate and detailed electronic documentation of work performed and results obtained.
  • Work independently as part of a team under direct supervision of a team lead.
  • Observe and comply with all safety standards and procedures.
Qualifications

Required Qualifications:

  • Associate Degree or College Diploma in Biology, Biochemistry, or a related scientific or engineering discipline.
  • Minimum of one (1) year of hands-on experience in a laboratory or biotechnology environment.
  • Demonstrated experience working with biomedical equipment, including routine maintenance, calibration, troubleshooting, and/or performance testing.

Strongly Preferred:

  • Experience with single-cell and spatial assay technologies. This includes familiarity with techniques such as single-cell RNA sequencing (scRNA-seq), spatial transcriptomics, multiplex imaging, or other high-dimensional molecular profiling platforms.
  • Working knowledge of sample preparation workflows, library preparation, quality control metrics, and data generation associated with next-generation sequencing or imaging-based assays.
  • Experience handling complex biological specimens and maintaining data integrity in high-throughput experimental environments.
  • Bachelor’s Degree in Biology, Biochemistry, or a related science or engineering field.

What Cedars-Sinai employees say

Pay

Benefits

Hours and flexibility

Workplace

Get the full story on Breakroom